DeviceClearance

Product code IQX— Physical Medicine

CAPP TERMINAL DEVICE

Classification name
Hook, External Limb Component, Mechanical
Device class
Class 1
Regulation
21 CFR 890.3420
Advisory panel
Physical Medicine
Total cleared
1
First cleared
Most recent

Market context for product code IQX

FDA has cleared 1 device under product code IQX, all in 1978, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code IQX

Recent clearances under product code IQX

Data sourced from openFDA. This site is unofficial and independent of the FDA.